The Maqsad area in the Oman ophiolite exposes a >300 m thick dunitic mantle-crust transition zone (DTZ) that developed above a mantle diapir. The Maqsad DTZ is primarily made of “pure” dunites ...(olivine with scattered chromite and chromite seams) and “impregnated” dunites, which exhibit a significant lithological variability, including various kinds of clinopyroxene-, plagioclase-, orthopyroxene-, amphibole (hornblende/pargasite)-bearing dunites. These minerals are interstitial between olivine grains and their variable abundance and distribution suggest that they crystallized from a percolating melt. Generally studied through in-situ mineral characterization, the whole rock composition of dunites is poorly documented. This study reports on whole rock and minerals major and trace element contents on 79 pure to variably impregnated dunites collected systematically along cross sections from the base to the top of the DTZ. In spite of its high degree of depletion, the olivine matrix is selectively enriched in the most incompatible trace elements such as LREE, HFSE, Th, U, Rb and Ba. These data support the view that this enrichment has been acquired early in the magmatic evolution of the DTZ, during the dunitization process itself. The dissolution of orthopyroxene from mantle harzburgites enhanced by the involvement of hydrothermal fluids produced low amounts of melts enriched in silica and in some trace elements that re-equilibrated with the olivine matrix. This pristine signature of the DTZ dunite was eventually variably altered by percolation of melts with a Mid-Ocean Ridge Basalt (MORB) affinity but displaying a wide spectrum of composition attributable to evolution by fractional crystallization and hybridization with the silica enriched, hydrated melts. The olivine matrix has been partially or fully re-equilibrated with these melts, smoothing the early strong concave-upward REE pattern in dunite. The chemical variability in the interstitial minerals bears witness of the percolation of MORB, issued from the mantle decompression melting, variably hybridized with melt batches produced within the DTZ by melt-rock reaction and poorly homogenized before reaching the lower crust. Our results lead to the conclusion that pure and impregnated dunites are end-members that recorded different stages of the same initial igneous processes: pure dunites are residues left after extraction of a percolating melt while impregnated dunites correspond to a stage frozen before complete melt extraction. Therefore dunites trace elements contents allow deciphering the multi-stage processes that led to their formation at the mantle-crust transition zone.
On Earth, most of the critical processes happen at the frontiers between envelopes and especially at the Moho between the mantle and the crust. Beneath oceanic spreading centers, the dunitic ...transition zone (DTZ) appears as a major interface between the upwelling and partially molten peridotitic mantle and the accreting gabbroic lower crust. Better constraints on the processes taking part in the DTZ allows improved understanding of the interactions between silicate melts and hydrated fluids, which act competitively to generate the petrological Moho. Here we combine mineral and whole rock major and trace element data with a structural approach along three cross-sections up to 300 m thick above the fossil Maqsad mantle diapir (Oman ophiolite) in order to understand the vertical organization of the DTZ with depth. Our results highlight that most of the faults or fractures cross-cutting the DTZ were ridge-related and active at an early, high temperature magmatic stage. Chemical variations along the cross-sections define trends with a characteristic vertical scale of few tens of meters. There is a clear correlation between the chemical variation pattern and the distribution of fault zones, not only for fluid-mobile elements but also for immobile elements such as REE and HFSE. Faults, despite displaying very limited displacements, enhanced both melt migration and extraction up to the crust and deep hydrothermal fluids introduction down to the Moho level. We propose that these faults are a vector for upwelling melt modification by hybridization, with hydrothermal fluids and/or silicic hydrous melts, and crystallization. Infiltration of these melts or fluids in the country rock governs part of the gradational evolutions recorded in composition of both the olivine matrix and interstitial phases away from faults. Finally, these faults likely control the thermal structure of the mantle-crust transition as evidenced by the spatial distribution of the crystallization products from percolating melts, organizing the transition zone into pure dunites to impregnated dunites horizons. In this context, the DTZ appears as a reactive interface that developed by the combination of three primary processes: tectonics, magmatism and deep, high temperature hydrothermal circulations. Accordingly, these features fundamentally contribute to the variable petrological and geochemical organization of the DTZ and possibly of the lower crust below oceanic spreading centers, and may be a clue to interpret part the heterogeneity observed in MORB signatures worldwide.
•The dunitic transition zone in the Oman ophiolite shows vertical chemical evolutions.•Syn-magmatic faults cut across the DTZ and influence chemical variations.•Melt-fluid-rock reactions within the DTZ are strongly controlled by faults.
A stratiform chromite ore body crops out in the lower part of the dunitic mantle-crust transition zone (DTZ) that developed at the top of a mantle diapir in the Maqsad area in the Oman ophiolite. It ...is made of layers ranging in thickness from a few mm to a maximum of 3 m, and in modal composition from massive to antinodular and disseminated ore. The ore body is about 50 m thick and its lateral extent does not exceed several hundred meters. The layering dips gently to the southeast, parallel to that of the overlying gabbroic cumulates. The chromite composition is typical of a MORB kindred - moderate XCr (100 × Cr/(Cr + Al) atomic ratio), ranging from 48 to 60, and relatively high TiO2 content, ranging from about 0.3 to 0.5 wt% -, a characteristic shared by most lithologies issued from the igneous activity of the Maqsad diapir. The silicate matrix is essentially made of slightly serpentinized olivine with minor clinopyroxene and rare pargasitic amphibole, orthopyroxene and garnet. This strongly contrasts with the nature of the mineral inclusions mostly made of the assemblage amphibole-orthopyroxene-mica, enclosed in the chromite grains and represented in abundance all along the ore body whatever the ore grade. The inclusions demonstrate the involvement of a silica- and water-rich melt and/or fluid, in addition to MORB, in the early stages of chromite crystallization. The chemical composition of chromite, silicate matrix, together with the one of silicate inclusions display well-defined evolutions vertically along the stratiform chromitite. At the scale of the ore body, the compositional trends are independent of the ore concentration but the major kinks in these trends are well-correlated with levels of magmatic breccias. This shows that abrupt chemical changes can be attributed to sudden melt ± fluids injection events followed mainly by melt-fluid-rock interaction and in a lesser extent by quieter evolution by fractional crystallization. At the thin section scale, second order chemical variations, essentially in the Mg# (100 × Mg/(Mg + Fe2+) atomic ratio) of chromite and Fo of olivine, are clearly attributable to re-equilibration between these two solid phases, possibly in the presence of an interstitial melt/fluid.
•The Maqsad dunitic transition zone (Oman ophiolite) hosts a stratiform chromitite.•The matrix (ol, cpx) strongly contrasts with silicate inclusions (opx, amph, mica).•Vertical chemical evolutions along the ore body correlate to magmatic breccias.•Melt injections (breccias) controlled the hybridization between contrasted melts.
A regional survey of alkaline springs in Oman and Ligurian ophiolites shows that the alkaline water compositions significantly vary from one ophiolite to the other and within the same ophiolite. The ...first‐order correlation between the Na (and K) and Cl concentrations points to fluid compositions only partly due to evaporation. The scatter around the evaporation line implies that Na and Cl may not be conservative during the alteration of the ultramafic rocks. Mg is almost entirely depleted at pH > 10.5 as a result of serpentine formation within the ultramafic body and of brucite (and minor hydrotalcite) precipitation at the springs. Ca accumulates in the high‐pH fluids and is consumed by Ca‐carbonate formation at the springs, by mixing with river waters or by the CO2 supply from the atmosphere. Thermodynamic calculations show that brucite saturation is reached at pH values around 10.5 which triggers major changes in the water composition. The waters evolve from a quartz‐saturated low‐pH continental environment to a brucite‐dominated high‐pH serpentinizing system at low temperature. The highest water salinities are found in springs located along the basal thrust plane of the ophiolite. The highest Al concentrations are found in some springs located on the crustal side of the mantle/crust boundary. This poses the question of the hydrologic pathways and of the role of the mineralogical composition of the altered formations.
Key Points
New temperature and composition of the alkaline waters
Brucite formation at pH 10.5 triggers major chemical and mineralogical changes
Relationship between the water compositions and the hydrologic pathways
We report on the mineralogical assemblages found in the hyperalkaline springs hosted on Liguria and Oman ophiolites based on exhaustive X‐ray diffraction and scanning electron microprobe analyses. In ...Liguria, hyperalkaline springs produce a thin brownish calcite precipitate that covers the bedrock due to the concomitant atmospheric CO2 uptake and neutralization of the hyperalkaline waters. No brucite and portlandite minerals are observed. The discharge of alkaline waters in Oman ophiolite forms white‐orange precipitates. Calcium carbonate minerals (calcite and/or aragonite) are the most abundant and ubiquitous precipitates and are produced by the same mechanism as in Liguria. This process is observed as a thin surface crust made of rhombohedral calcite. Morphological features of aragonite vary from needle‐, bouquet‐, dumbbell‐, spheroidal‐like habitus according to the origin of carbon, temperature, and ionic composition of the hyperalkaline springs, and the biochemical and organic compounds. Brucite is observed both at hyperalkaline springs located at the thrust plane and at the paleo‐Moho. The varying mixing proportions between the surface runoff waters and the hyperalkaline ones control brucite precipitation. The layered double hydroxide minerals occur solely in the vicinity of hyperalkaline springs emerging within the bedded gabbros. Finally, the dominant mineralogical associations we found in Oman (Ca‐bearing carbonates and brucite) in a serpentinizing environment driven by the meteoric waters are surprisingly the same as those observed at the Lost City hydrothermal site in a totally marine environment.
Key Points
Distinct mineralogical association between Oman and liguria alkaline springs
There is no Mg‐bearing carbonate
similar mineral assemblage in marine and surface serpentinizing environment
•We use isotope geochemistry, geochronology and modelling of REE diffusion timescale.•Cabo Ortegal pyroxenites record Cadomian arc magmatism off a pre-Gondwanan block.•Melt–rock interaction occurred ...during the reworking of a rifted continental margin.•Subduction metasomatism and metamorphism obscure the age of orogenic mantle rocks.•2nd-stage Nd model ages may provide robust time constraints on pyroxenite formation.
Pyroxenites exposed in ophiolites and orogenic peridotite massifs may record petrogenetic processes occurring in mantle domains generated and/or transferred in supra-subduction environments. However, the timing of their formation and the geochemical characteristics of their source region commonly are obscured by metamorphic and metasomatic overprints. This is especially critical in arc-related environments, where pyroxenites may be formed during the differentiation of primitive magmas. Our approach combines Sr- and Nd-isotope geochemistry and geochronology, and modelling of REE diffusion, to further constrain the origin of a well-characterized set of pyroxenites from the arc-related Cabo Ortegal Complex, Spain. In the light of petrological constraints, Sr- and Nd-isotope systematics consistently indicate that cpx and amphibole have acquired disequilibrium during two main episodes: (1) a magmatic/metasomatic episode that led to the formation of the pyroxenites, coeval with that of Cabo Ortegal granulites and corresponding to the incipient stage of a potential Cadomian arc (459–762 Ma; isochron and second-stage Nd model ages); (2) an episode of metamorphic amphibolitization upon the percolation of relatively unradiogenic and LREE-enriched hydrous fluids, subsequent to the delamination of the pyroxenites from their arc-root settings during Devonian subduction. Calculations of diffusional timescale for the re-equilibration of REE are consistent with this scenario but provide only poor additional constraints due to the sensitivity of this method to grain size and sub-solidus temperature. We thus emphasize the necessity to combine isochron ages and Nd model ages corrected for radiogenic ingrowth to put time constraints on the formation of subduction- and/or collision-related pyroxenites, along with petrological and geochemical constraints. Homogeneous age-corrected 143Nd/144Nd of 0.5121–0.5125 (εNd between 0 and +7.5) and 87Sr/86Sr of 0.7037–0.7048 provide information on the sources of the metasomatic agents involved (and potentially the parental melts) and notably indicate the contributions from enriched mantle components (EM I and/or II). This suggests the involvement of an old crustal component, which is consistent with the derivation of the pyroxenites and granulites from an ensialic island arc, potentially built on the northern margin of either Gondwana or a pre-Gondwanan continental block. This case study thus documents the role of melt–rock reactions as major pyroxenite-forming processes in the sub-arc mantle, providing further constraints on their sources and timing in the Cabo Ortegal Complex.
The Bahla massif exposes the lower crustal section of the Oman ophiolite located close to the thrust front of the Semail nappe. It is affected by intense faulting previously attributed to tectonic ...events that dismembered a classical ophiolitic sequence during or after the obduction. Here we show that most of this complexity is primary, inherited from syn-accretion tectonics. The crustal section is exposed in a 15 by 8 km tectonic enclave surrounded by mantle peridotite. Its northern boundary corresponds to a major, steeply dipping normal fault striking WNW-ESE, at low angle to the paleo-ridge axis. Movement along this fault was accommodated by intense plastic deformation of the crustal cumulates and adjacent mantle peridotites at temperature conditions ≥900 °C. The thickness of the deformed zone reaches several hundred meters. The flattening of the cumulate layering away from the fault is correlated to a decrease in the deformation intensity. Undeformed olivine-gabbro dykes cross-cut this “tectonic Moho” indicating that the tilting occurred before the end of the igneous activity. To the southwest, the crustal enclave is bounded by a NW-SE trending transtentional shear zone that was active in the amphibolite to greenschist facies and was intensely injected by syn- to post-kinematic gabbronorite and tonalite/trondhjemite dykes and plugs. The age of one felsic sample (95.214 ± 0.032 Ma, high-precision UPb zircon dating) is within error of the age of intrusive felsic intrusions into the mantle and lowermost axial crust from the length of the Oman ophiolite, which slightly post-dates the mean crystallization age of the Semail crust (V1 magmatism; 96.1–95.6 Ma). Other contacts are low temperature features including cataclastic faults, serpentine‑carbonate breccias and flat-lying décollements.
Parent melts of the Bahla crustal cumulates were more siliceous and hydrous, i.e. more andesitic, than typical mid-ocean ridge basalt (MORB) as deduced from the frequent occurrence of early crystallizing orthopyroxene (opx) and late crystallizing amphibole. Some facies such as cumulate harzburgite and opx-troctolite have not been documented elsewhere in the Oman ophiolite and may be specific to the tectonic context in which the frontal massifs accreted. The chemical composition of the lower crustal cumulates can be accounted for by the hybridization in various proportions between MORB and a primitive andesite from a depleted source whose origin can be looked for in melts from a nascent subduction zone or from high temperature hydrothermal processes.
The structure of the Bahla lower crustal section is reminiscent of the plutonic growth faults documented along present-day slow-spreading centres in both mid-ocean ridge and back arc settings. The distinctive characteristics of the Moho and lower crustal section in the Bahla massif are tentatively related to their position at the leading edge of the ophiolite, i.e. closer to the Arabian continental margin at the time of accretion than the massifs from the internal part of the ophiolite that have a more continuous and less deformed lower crust. It indicates that the style of crustal accretion may have changed during the opening of the oceanic basin from which the Oman ophiolite issued.
•The Bahla massif crops out along the thrust front of the Oman ophiolite.•Its crustal section presents distinctive structural and petrological features contrasting with the ones of most other Oman massifs.•It is affected by intense faulting inherited from syn-accretion tectonics and/or from the very early stage of intra-oceanic thrusting.•Some lithological facies from the lower crustal cumulates seem specific to the frontal massifs and are attributable to magma mixing and contamination by hydrous fluids.•Our results highlight the heterogeneity of the Oman ophiolite.•The paradigm considering the Oman ophiolite as a whole the archetype of ocean lithosphere accreted in a fast-spreading setting should be nuanced.
Mantle lithologies in orogenic massifs and xenoliths commonly display strikingly different Hf- and Nd-isotope compositions compared to oceanic basalts. While the presence of pyroxenites has long been ...suggested in the source region of mantle-derived magmas, very few studies have reported their combined HfNd isotope compositions. We here report the first LuHf data along with ReOs data and S concentrations on the Cabo Ortegal Complex, where the pyroxenite-rich Herbeira massif has been interpreted as remnants of a delaminated arc root. The pyroxenites, chromitites and their host harzburgites show a wide range of whole-rock 187Re/188Os and 187Os/188Os (0.16–1.44), indicating that Re was strongly mobilized, partly during hydrous retrograde metamorphism but mostly during supergene alteration that preferentially affected low-Mg#, low Cu/S pyroxenites. Samples that escaped this disturbance yield an isochron age of 838 ± 42 Ma, interpreted as the formation of Cabo Ortegal pyroxenites. Corresponding values of initial 187Os/188Os (0.111–0.117) are relatively unradiogenic, suggesting limited contributions of slab-derived Os to primitive arc melts such as those parental to these pyroxenites. This interpretation is consistent with radiogenic Os in arc lavas being mostly related to crustal assimilation. Paleoproterozoic to Archean Os model ages confirm that Cabo Ortegal pyroxenites record incipient volcanic arc magmatism on the continental margin of the Western African Craton, as notably documented by zircon UPb ages of 2.1 and 2.7 Ga. LuHf data collected on clinopyroxene and amphibole separates and whole-rock samples are characterized by uncorrelated 176Lu/177Hf and 176Hf/177Hf (0.2822–0.2855), decoupled from Nd-isotope compositions. This decoupling is ascribed to diffusional disequilibrium during melt-peridotite interaction, in good agreement with the results of percolation-diffusion models simulating the interaction of an arc melt with an ancient melt-depleted residue. These models notably show that HfNd isotopic decoupling such as recorded by Cabo Ortegal pyroxenites and peridotites (ΔƐHf(i) up to +97) is enhanced during melt-peridotite interaction by slow diffusional re-equilibration and can be relatively insensitive to chromatographic fractionation. Finally, we discuss the hypothesis that arc-continent interaction may provide preferential conditions for such isotopic decoupling and propose that its ubiquitous recognition in peridotites reflects the recycling of sub-arc mantle domains derived from ancient, reworked SCLM.
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